Li Huanyu, Liu Ting, He Yinna, Song Jiangnan, Meng Alan, Sun Changlong, Hu Minmin, Wang Lei, Li Guicun, Zhang Zhenhui, Liu Yuan, Zhao Jian, Li Zhenjiang
College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, Shandong, P. R. China.
Key Laboratory of Polymer Material Advanced Manufacturing Technology of Shandong Provincial, College of Electromechanical Engineering, Qingdao University of Science and Technology, Qingdao 266061, Shandong, P. R. China.
ACS Appl Mater Interfaces. 2022 Jan 19;14(2):3363-3373. doi: 10.1021/acsami.1c17356. Epub 2022 Jan 5.
Developing novel hybrid negative electrode materials with high specific capacity, rate capacitance, and long-term cycle stability is a key factor for pushing large-scale application of supercapacitors. However, construction of robust interfaces and low-crystalline active materials plays a crucial role in realizing the target. In this paper, a one-step phosphorization approach was employed to make low-crystalline FePO nanoplates closely bonded to N/P-co-doped graphene nanotubes (N/P-GNTs@b-FePO) through interfacial chemical bonding. The N and P heteroatoms as substitutions for C in GNT skeletons can introduce rich electronic centers, which induces FePO to fix the surface of N/P-GNTs through Fe-N and Fe-P bonds as confirmed by the characterizations. Moreover, the low-crystalline active materials own a disordered internal structure and numerous defects, which not only endows with excellent conductivity but also provides many active sites for redox reactions. Benefiting from the synergistic effects, the prepared N/P-GNTs@b-FePO can not only deliver a high capacity of 257 mA h g (927 F g) at 1 A g but also present an excellent rate capability of 184 mA h g (665 F g) at 50 A g and outstanding cycle stability (∼90.6% capacity retention over 40,000 cycles). Furthermore, an asymmetric supercapacitor was assembled using the obtained N/P-GNTs@b-FePO as electrode materials, which can present the energy density as high as 83.3 W h kg at 791 W kg and long-term durability. Therefore, this strategy not only offers an effective pathway for achieving high-performance negative electrode materials but also lays a foundation for further industrialization.
开发具有高比容量、倍率电容和长期循环稳定性的新型混合负极材料是推动超级电容器大规模应用的关键因素。然而,构建坚固的界面和低结晶度的活性材料在实现这一目标中起着至关重要的作用。本文采用一步磷化法,通过界面化学键合使低结晶度的磷酸铁纳米片与氮/磷共掺杂的石墨烯纳米管(N/P-GNTs@b-FePO)紧密结合。作为石墨烯纳米管骨架中碳的替代物,氮和磷杂原子可引入丰富的电子中心,经表征证实,这会促使磷酸铁通过铁-氮键和铁-磷键固定在氮/磷-石墨烯纳米管表面。此外,低结晶度的活性材料具有无序的内部结构和大量缺陷,这不仅赋予其优异的导电性,还为氧化还原反应提供了许多活性位点。得益于协同效应,制备的N/P-GNTs@b-FePO不仅在1 A g时能提供257 mA h g(927 F g)的高容量,而且在50 A g时具有184 mA h g(665 F g)的优异倍率性能和出色的循环稳定性(在40000次循环中容量保持率约为90.6%)。此外,以所得的N/P-GNTs@b-FePO作为电极材料组装了一个不对称超级电容器,其在791 W kg时的能量密度高达83.3 W h kg,且具有长期耐久性。因此,该策略不仅为实现高性能负极材料提供了一条有效途径,也为进一步的工业化奠定了基础。